Canonical Allele Identifier: CA1077368978
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs1748651530
gnomAD v3: 5-71719236-GGGCTCACTATAAAAGGTGGGAGCGCGT-G
gnomAD v4: 5-71719236-GGGCTCACTATAAAAGGTGGGAGCGCGT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719239_71719265del , CM000667.2:g.71719239_71719265del GRCh38
NC_000005.9:g.71015066_71015092del , CM000667.1:g.71015066_71015092del GRCh37
NC_000005.8:g.71050822_71050848del NCBI36
NG_015988.1:g.5077_5103del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-55_-29del ENSP00000296777.4:n.-55_-29del
NM_004291.3:c.-55_-29del NP_004282.1:n.-55_-29del
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